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Fc介导的免疫球蛋白G与血管内皮细胞中波形蛋白型中间丝的结合。

Fc-mediated binding of IgG to vimentin-type intermediate filaments in vascular endothelial cells.

作者信息

Hansson G K, Starkebaum G A, Benditt E P, Schwartz S M

出版信息

Proc Natl Acad Sci U S A. 1984 May;81(10):3103-7. doi: 10.1073/pnas.81.10.3103.

Abstract

Prior studies have shown that vascular endothelial cells bind circulating IgG intracellularly during cell death. We now demonstrate that all endothelial cells have intracellular binding sites for IgG and that these binding sites are exposed to circulating IgG only if the plasma membrane is damaged. The binding sites are located on the cytoskeletal intermediate filaments and can be detected also in other cells containing vimentin-type intermediate filaments. Monoclonal human IgG1 exhibited saturable, high-affinity binding to vimentin-enriched cytoskeletons. Binding was inhibited by Fc fragments but not by Fab, F(ab')2, or pFc' fragments, suggesting that the binding site on IgG is located in the C gamma 2 domain of the Fc fragment. Binding of IgG to intermediate filaments may be important for the destruction and removal of damaged cells.

摘要

先前的研究表明,血管内皮细胞在细胞死亡过程中会在细胞内结合循环中的免疫球蛋白G(IgG)。我们现在证明,所有内皮细胞都有IgG的细胞内结合位点,并且只有当质膜受损时,这些结合位点才会暴露于循环中的IgG。这些结合位点位于细胞骨架中间丝上,在其他含有波形蛋白型中间丝的细胞中也能检测到。单克隆人IgG1对富含波形蛋白的细胞骨架表现出饱和、高亲和力的结合。Fc片段可抑制结合,但Fab、F(ab')2或pFc'片段则不能,这表明IgG上的结合位点位于Fc片段的Cγ2结构域。IgG与中间丝的结合可能对受损细胞的破坏和清除很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2459/345229/826dd9cb7ad8/pnas00611-0167-a.jpg

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